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Completed Phase 2 Interventional Results available

Safety Study to Assess IV Zanamivir for Treatment of Influenza Infection in Patients Who Are in Hospital

ClinicalTrials.gov ID: NCT01014988

Public ClinicalTrials.gov record NCT01014988. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 5, 2026, 10:22 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-label, Multi-center, Single Arm Study to Evaluate the Safety and Tolerability of Intravenous Zanamivir in the Treatment of Hospitalized Adult, Adolescent and Pediatric Subjects With Confirmed Influenza Infection

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine whether zanamivir aqueous solution given by intravenous injection is safe in treating hospitalized patients with confirmed influenza infection. A single arm open-label design has been selected to achieve the primary objective of providing regulatory authorities with safety data on IV zanamivir.

Study identification

NCT ID
NCT01014988
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
202 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
6 Months and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2009 (Type not available)
Primary completion
Feb 2015 (Actual)
Completion
Feb 2015 (Actual)
Last update posted
Mar 28, 2017

2009 – 2015

United States locations

U.S. sites
40
U.S. states
27
U.S. cities
36
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35233 —
GSK Investigational Site Phoenix Arizona 85023 —
GSK Investigational Site Little Rock Arkansas 72202 —
GSK Investigational Site San Diego California 92123 —
GSK Investigational Site Stamford Connecticut 06902 —
GSK Investigational Site Washington D.C. District of Columbia 20007 —
GSK Investigational Site Washington D.C. District of Columbia 20010 —
GSK Investigational Site Gainesville Florida 32608 —
GSK Investigational Site Tampa Florida 33606 —
GSK Investigational Site Atlanta Georgia 30322 —
GSK Investigational Site Decatur Georgia 30033 —
GSK Investigational Site Indianapolis Indiana 46202 —
GSK Investigational Site Topeka Kansas 66604 —
GSK Investigational Site Louisville Kentucky 40202 —
GSK Investigational Site New Orleans Louisiana 70112 —
GSK Investigational Site Boston Massachusetts 02115-5724 —
GSK Investigational Site Boston Massachusetts 02115 —
GSK Investigational Site Saint Paul Minnesota 55102 —
GSK Investigational Site Kansas City Missouri 64108 —
GSK Investigational Site St Louis Missouri 63110 —
GSK Investigational Site Butte Montana 59701 —
GSK Investigational Site Camden New Jersey 08103 —
GSK Investigational Site New Hyde Park New York 11040 —
GSK Investigational Site Chapel Hill North Carolina 27514 —
GSK Investigational Site Charlotte North Carolina 28203 —
GSK Investigational Site Cleveland Ohio 44106 —
GSK Investigational Site Columbus Ohio 43205 —
GSK Investigational Site Toledo Ohio 43606 —
GSK Investigational Site Portland Oregon 97239 —
GSK Investigational Site Philadelphia Pennsylvania 19102 —
GSK Investigational Site Pittsburgh Pennsylvania 15224 —
GSK Investigational Site Memphis Tennessee 38103 —
GSK Investigational Site Memphis Tennessee 38105 —
GSK Investigational Site Dallas Texas 75231 —
GSK Investigational Site Dallas Texas 75235 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Salt Lake City Utah 84113 —
GSK Investigational Site Richmond Virginia 23249 —
GSK Investigational Site Milwaukee Wisconsin 53201 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 70 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01014988, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 28, 2017 · Synced Nov 5, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01014988 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →